132434-56-1

Basic information

• Product Name: 1,3-bis(3-nitrophenyl)-2-propen-1-one
• Synonyms: 1,3-bis(3-nitrophenyl)-2-propen-1-one
• CAS NO: 132434-56-1
• Molecular Weight: 298.255
• Mol File: 132434-56-1.mol

Chemical Properties

• CAS DataBase Reference: 1,3-bis(3-nitrophenyl)-2-propen-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-bis(3-nitrophenyl)-2-propen-1-one(132434-56-1)
• EPA Substance Registry System: 1,3-bis(3-nitrophenyl)-2-propen-1-one(132434-56-1)

Safety Data

• Hazardous Substances Data: 132434-56-1(Hazardous Substances Data)

Upstream product

• 99-61-6 3-nitro-benzaldehyde 
• 121-89-1 3-Nitroacetophenone 

Downstream Products

• 23916-05-4 3,3'-propane-1,3-diyldianiline 
• 106523-28-8 1,3-bis(3'-nitrophenyl)-1,3-propanedione 
• 175027-43-7 C₃₁H₂₂N₂O₇ 
• 53290-50-9 2,3-dibromo-1,3-bis-(3-nitro-phenyl)-propan-1-one 

Relevant articles and documents

MACROCYCLIC COMPOUNDS AND THEIR USE AS KINASE INHIBITORS

The present invention relates to macrocyclic compounds of Formula I: or pharmaceutically acceptable salts thereof or quaternary ammonium salts thereof wherein constituent members are provided hereinwith, as well as their compositions and methods of use, w

Synthesis and antifungal activity of 1,3-bis(4-methyl/4-bromo/3-nitrophenyl) propan-1,3-diones and their 2 analogs

The reaction of substituted acetophenones (1-3) with 4-methyl-, 4-bromo- or 3-nitrobenzaldehyde (4-6) in ethanolic NaOH gives the correponding 1,3-bis(4-methyl/4-bromo/3-nitrophenyl)-2-propen-1-ones (7-9) in good yields, which on bromination yield substit

Photochemical Reactions of Phthalamido Derivatives of 1,3-Diphenyl-2-propen-1-one and Its Analogs

According to luminescence spectral data, the singlet excited state of 1,4-bis(3-aryl-3-oxo-1-propenyl)benzene derivatives is of ?, ?* type, whereas those of 1,3-diaryl-2-propen-1-ones and 1,4-bis(3-phenyl-2-propenoyl)benzene are of n, ?* type.When irradiated in solutions in alcohol, CDCl3, or tetrahydrofuran, these compounds undergo photochemical isomerization and cacloaddition and react with oxygen.As follows from the quantum yields, photoisomerization is the predominant process for 1,3-diaryl-2-propen-1-ones and 1,4-bis(3-phenyl-2-propenoyl)benzene, whereas for 1,4-bis(3-aryl-3-oxo-1-propenyl)benzenes the main route is cycloaddition; the efficiency of these photochemical conversions decreases in going from the two first compounds to the latter.Presumably, one of the reasons is the different reactive excited states.